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Periodontal inflamed surface area and C-reactive protein as predictors of HbA1c: a study in Indonesia

Periodontitis may exert an infectious and inflammatory burden, evidenced by increased C-reactive protein (CRP). This burden may impair blood glucose control (HbA1c). The aim of our study was to analyze whether periodontitis severity as measured with the periodontal inflamed surface area (PISA) and C...

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Autores principales: Susanto, Hendri, Nesse, Willem, Dijkstra, Pieter U., Hoedemaker, Evelien, van Reenen, Yvonne Huijser, Agustina, Dewi, Vissink, Arjan, Abbas, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3400038/
https://www.ncbi.nlm.nih.gov/pubmed/22012468
http://dx.doi.org/10.1007/s00784-011-0621-0
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author Susanto, Hendri
Nesse, Willem
Dijkstra, Pieter U.
Hoedemaker, Evelien
van Reenen, Yvonne Huijser
Agustina, Dewi
Vissink, Arjan
Abbas, Frank
author_facet Susanto, Hendri
Nesse, Willem
Dijkstra, Pieter U.
Hoedemaker, Evelien
van Reenen, Yvonne Huijser
Agustina, Dewi
Vissink, Arjan
Abbas, Frank
author_sort Susanto, Hendri
collection PubMed
description Periodontitis may exert an infectious and inflammatory burden, evidenced by increased C-reactive protein (CRP). This burden may impair blood glucose control (HbA1c). The aim of our study was to analyze whether periodontitis severity as measured with the periodontal inflamed surface area (PISA) and CRP predict HbA1c levels in a group of healthy Indonesians and a group of Indonesians treated for type 2 diabetes mellitus (DM2). A full-mouth periodontal examination, including probing pocket depth, gingival recession, clinical attachment loss, plaque index and bleeding on probing, was performed in 132 healthy Indonesians and 101 Indonesians treated for DM2. Using these data, PISA was calculated. In addition, HbA1c and CRP were analyzed. A validated questionnaire was used to assess smoking, body mass index (BMI), education and medical conditions. In regression analyses, it was assessed whether periodontitis severity and CRP predict HbA1c, controlling for confounding and effect modification (i.e., age, sex, BMI, pack years, and education). In healthy Indonesians, PISA and CRP predicted HbA1c as did age, sex, and smoking. In Indonesians treated for DM2, PISA did not predict HbA1c. Periodontitis may impair blood glucose regulation in healthy Indonesians in conjunction with elevated CRP levels. The potential effect of periodontitis on glucose control in DM2 patients may be masked by DM2 treatment. Clinical relevance: periodontitis may impair blood glucose control through exerting an inflammatory and infectious burden evidenced by increased levels of CRP.
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spelling pubmed-34000382012-07-25 Periodontal inflamed surface area and C-reactive protein as predictors of HbA1c: a study in Indonesia Susanto, Hendri Nesse, Willem Dijkstra, Pieter U. Hoedemaker, Evelien van Reenen, Yvonne Huijser Agustina, Dewi Vissink, Arjan Abbas, Frank Clin Oral Investig Original Article Periodontitis may exert an infectious and inflammatory burden, evidenced by increased C-reactive protein (CRP). This burden may impair blood glucose control (HbA1c). The aim of our study was to analyze whether periodontitis severity as measured with the periodontal inflamed surface area (PISA) and CRP predict HbA1c levels in a group of healthy Indonesians and a group of Indonesians treated for type 2 diabetes mellitus (DM2). A full-mouth periodontal examination, including probing pocket depth, gingival recession, clinical attachment loss, plaque index and bleeding on probing, was performed in 132 healthy Indonesians and 101 Indonesians treated for DM2. Using these data, PISA was calculated. In addition, HbA1c and CRP were analyzed. A validated questionnaire was used to assess smoking, body mass index (BMI), education and medical conditions. In regression analyses, it was assessed whether periodontitis severity and CRP predict HbA1c, controlling for confounding and effect modification (i.e., age, sex, BMI, pack years, and education). In healthy Indonesians, PISA and CRP predicted HbA1c as did age, sex, and smoking. In Indonesians treated for DM2, PISA did not predict HbA1c. Periodontitis may impair blood glucose regulation in healthy Indonesians in conjunction with elevated CRP levels. The potential effect of periodontitis on glucose control in DM2 patients may be masked by DM2 treatment. Clinical relevance: periodontitis may impair blood glucose control through exerting an inflammatory and infectious burden evidenced by increased levels of CRP. Springer-Verlag 2011-10-20 2012 /pmc/articles/PMC3400038/ /pubmed/22012468 http://dx.doi.org/10.1007/s00784-011-0621-0 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Article
Susanto, Hendri
Nesse, Willem
Dijkstra, Pieter U.
Hoedemaker, Evelien
van Reenen, Yvonne Huijser
Agustina, Dewi
Vissink, Arjan
Abbas, Frank
Periodontal inflamed surface area and C-reactive protein as predictors of HbA1c: a study in Indonesia
title Periodontal inflamed surface area and C-reactive protein as predictors of HbA1c: a study in Indonesia
title_full Periodontal inflamed surface area and C-reactive protein as predictors of HbA1c: a study in Indonesia
title_fullStr Periodontal inflamed surface area and C-reactive protein as predictors of HbA1c: a study in Indonesia
title_full_unstemmed Periodontal inflamed surface area and C-reactive protein as predictors of HbA1c: a study in Indonesia
title_short Periodontal inflamed surface area and C-reactive protein as predictors of HbA1c: a study in Indonesia
title_sort periodontal inflamed surface area and c-reactive protein as predictors of hba1c: a study in indonesia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3400038/
https://www.ncbi.nlm.nih.gov/pubmed/22012468
http://dx.doi.org/10.1007/s00784-011-0621-0
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